Variant report

Variant	rs35249036
Chromosome Location	chr6:26026163-26026164
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:26024607..26035097-chr6:27857610..27864739,17	K562	blood:
2	chr6:25903958..25905764-chr6:26024857..26026815,2	K562	blood:
3	chr22:21354576..21357139-chr6:26025887..26028431,2	K562	blood:
4	chr6:26024260..26027949-chr6:26272859..26275159,3	MCF-7	breast:
5	chr1:33116434..33118067-chr6:26025894..26027633,2	MCF-7	breast:
6	chr6:26026024..26027759-chr6:26164190..26165983,2	MCF-7	breast:
7	chr6:26025967..26028344-chr6:26231112..26233437,2	MCF-7	breast:
8	chr6:25725904..25728723-chr6:26024464..26030208,7	K562	blood:
9	chr6:26022756..26026190-chr6:26183005..26186257,3	MCF-7	breast:
10	chr6:26017750..26036418-chr6:26116875..26130553,65	MCF-7	breast:
11	chr20:10412792..10415646-chr6:26026013..26027759,2	MCF-7	breast:
12	chr6:25868103..25870310-chr6:26025441..26027825,2	K562	blood:
13	chr6:26026035..26027624-chr6:27806330..27807928,2	K562	blood:
14	chr6:26025218..26027872-chr6:27113164..27115614,4	MCF-7	breast:
15	chr6:26024741..26028835-chr6:26213584..26218792,8	MCF-7	breast:
16	chr16:14165034..14167811-chr6:26024913..26027065,2	MCF-7	breast:
17	chr6:25991732..25993497-chr6:26025765..26028422,2	MCF-7	breast:
18	chr6:26026020..26027714-chr6:27113158..27114854,2	K562	blood:
19	chr17:79826225..79829012-chr6:26026159..26027799,2	K562	blood:
20	chr15:65587818..65589670-chr6:26025998..26027787,2	MCF-7	breast:
21	chr6:16128760..16131602-chr6:26025170..26028391,3	K562	blood:
22	chr6:26025221..26028451-chr6:27796635..27801025,4	K562	blood:
23	chr6:26024161..26035534-chr6:27093020..27104638,25	K562	blood:
24	chr6:26025403..26028129-chr6:27797100..27800385,4	MCF-7	breast:
25	chr6:26019620..26034082-chr6:26100355..26110400,33	MCF-7	breast:
26	chr6:26025188..26029060-chr6:27836295..27841543,4	MCF-7	breast:
27	chr6:17705633..17708483-chr6:26025891..26028298,2	K562	blood:
28	chr6:26025697..26028574-chr6:27100456..27102922,3	MCF-7	breast:
29	chr6:25724700..25728805-chr6:26024464..26033486,16	K562	blood:
30	chr6:26025755..26029009-chr6:27774713..27777489,4	MCF-7	breast:
31	chr6:26026115..26036040-chr6:27097153..27104835,26	K562	blood:
32	chr6:17705633..17707501-chr6:26024961..26027391,2	K562	blood:
33	chr6:26024574..26026765-chr6:27779935..27784258,4	MCF-7	breast:
34	chr11:65268214..65271270-chr6:26025584..26028816,3	K562	blood:
35	chr6:26019525..26036768-chr6:26154463..26163826,38	MCF-7	breast:
36	chr6:25770868..25773858-chr6:26023960..26026372,2	K562	blood:
37	chr17:60500257..60502888-chr6:26024966..26026833,2	MCF-7	breast:
38	chr1:45186114..45187796-chr6:26023695..26026334,2	K562	blood:
39	chr6:24718870..24722603-chr6:26025035..26028594,6	K562	blood:
40	chr6:26025957..26026618-chr6:38670452..38671374,2	Hela-S3	cervix:
41	chr6:16128760..16130953-chr6:26025170..26027575,2	K562	blood:
42	chr6:26023233..26029617-chr6:27098032..27102736,8	MCF-7	breast:
43	chr6:25715103..25717600-chr6:26025342..26027006,2	K562	blood:
44	chr6:26025174..26027343-chr6:44222131..44224578,2	K562	blood:
45	chr6:26025156..26026780-chr6:26198684..26200842,3	MCF-7	breast:
46	chr6:26024775..26027574-chr6:27806170..27808884,2	MCF-7	breast:
47	chr12:125397798..125400421-chr6:26024169..26027014,2	K562	blood:
48	chr6:26025653..26028340-chr6:27857674..27861144,4	MCF-7	breast:
49	chr6:26025629..26034912-chr6:27111740..27118591,16	K562	blood:
50	chr6:25815670..25817805-chr6:26023772..26026726,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000197846	Chromatin interaction
ENSG00000198558	Chromatin interaction
ENSG00000168242	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000162521	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000218281	Chromatin interaction
ENSG00000175711	Chromatin interaction
ENSG00000217159	Chromatin interaction
ENSG00000272462	Chromatin interaction
ENSG00000176261	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000124789	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000125863	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000265345	Chromatin interaction
ENSG00000087995	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000141522	Chromatin interaction
ENSG00000146047	Chromatin interaction
ENSG00000230513	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000124767	Chromatin interaction
ENSG00000007944	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000124564	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000197061	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000197914	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000186260	Chromatin interaction
ENSG00000150991	Chromatin interaction
ENSG00000182572	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000272269	Chromatin interaction
ENSG00000112308	Chromatin interaction
ENSG00000187475	Chromatin interaction
ENSG00000164508	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000199568	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs1045537	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484433	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484435	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13191776	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13192365	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13192713	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13193424	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13195279	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13195692	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13196552	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13197334	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13200797	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13200888	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13201821	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13202371	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13203673	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13206443	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13206501	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13207673	0.82[EUR][1000 genomes]
rs13210399	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13212652	0.86[EUR][1000 genomes]
rs13214280	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13216785	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13220395	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13220488	0.82[EUR][1000 genomes]
rs16891235	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891261	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16891264	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16891315	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891334	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17586553	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17586784	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17587597	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2051539	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360595	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34027471	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34116162	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34233736	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34391493	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34791189	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34804024	0.84[AMR][1000 genomes]
rs35069699	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35116528	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35169013	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35335639	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35367169	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35378061	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35402046	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35484309	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35528636	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35778245	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35825164	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35902160	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36012762	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3734523	0.81[ASN][1000 genomes]
rs3734528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3752417	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56195001	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56294283	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60512607	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66790453	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67296946	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67844427	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs68149500	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6931120	0.81[ASN][1000 genomes]
rs6940007	0.81[ASN][1000 genomes]
rs71557315	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71557316	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72832596	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72834617	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72834623	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7749414	1.00[ASN][1000 genomes]
rs9295675	0.81[ASN][1000 genomes]
rs9461223	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
14	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
15	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
16	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs35249036	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL
rs35249036	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26022200-26026600	Weak transcription	Spleen	Spleen
2	chr6:26022200-26026800	Weak transcription	Gastric	stomach
3	chr6:26022400-26026200	Weak transcription	Brain Angular Gyrus	brain
4	chr6:26022400-26026200	Weak transcription	Fetal Brain Male	brain
5	chr6:26022400-26026400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:26022400-26026600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:26022400-26026800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:26022600-26026200	Weak transcription	Brain Substantia Nigra	brain
9	chr6:26022600-26026200	Weak transcription	Right Atrium	heart
10	chr6:26022600-26026400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:26022800-26026200	Weak transcription	Brain Hippocampus Middle	brain
12	chr6:26022800-26026200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:26023000-26026200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:26023000-26026200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr6:26023000-26026200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:26023000-26026200	Enhancers	Fetal Thymus	thymus
17	chr6:26023400-26026200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr6:26023400-26026400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr6:26024600-26026200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:26024600-26026200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:26024600-26026200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:26024800-26026200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:26024800-26026200	Enhancers	NHLF	lung
24	chr6:26024800-26026400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:26024800-26026400	Enhancers	Fetal Heart	heart
26	chr6:26025000-26026200	Enhancers	Colon Smooth Muscle	Colon
27	chr6:26025200-26026200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr6:26025200-26026200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:26025200-26026200	Enhancers	Fetal Intestine Large	intestine
30	chr6:26025200-26026200	Enhancers	Rectal Smooth Muscle	rectum
31	chr6:26025200-26026400	Enhancers	Stomach Mucosa	stomach
32	chr6:26025400-26026200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr6:26025400-26026200	Enhancers	Aorta	Aorta
34	chr6:26025400-26026200	Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr6:26025600-26026200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr6:26025600-26026200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr6:26025600-26026200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:26025600-26026200	Enhancers	Primary B cells from peripheral blood	blood
39	chr6:26025600-26026200	Enhancers	Primary T cells fromperipheralblood	blood
40	chr6:26025600-26026200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr6:26025600-26026200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr6:26025600-26026200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:26025600-26026200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr6:26025600-26026200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:26025600-26026200	Enhancers	Fetal Muscle Leg	muscle
46	chr6:26025600-26026200	Enhancers	HSMM	muscle
47	chr6:26025600-26026200	Enhancers	HSMMtube	muscle
48	chr6:26025600-26026200	Enhancers	NHDF-Ad	bronchial
49	chr6:26025600-26026400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr6:26025600-26026400	Enhancers	Primary monocytes fromperipheralblood	blood

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