Variant report

Variant	rs35965384
Chromosome Location	chr19:21933464-21933465
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21933459-21933509	AG09309	skin:	n/a
2	chr19:21933455-21933505	HNPCEpiC	eye:	n/a
3	chr19:21933455-21933505	HRCEpiC	kidney:	n/a
4	chr19:21933455-21933505	AG04450	lung:	fetal
5	chr19:21933455-21933505	GM19239	blood:	n/a
6	chr19:21933450-21933500	ovcar-3	ovarian:	n/a
7	chr19:21933459-21933509	LNCaP	prostate:	n/a
8	chr19:21933459-21933509	AG10803	skin:	n/a
9	chr19:21933455-21933505	RPTEC	kidney:	n/a
10	chr19:21933455-21933505	IMR90	lung:	fetal
11	chr19:21933455-21933505	HAEpiC	amniotic membrane:	n/a
12	chr19:21933459-21933509	IMR90	lung:	fetal
13	chr19:21933459-21933509	ovcar-3	ovarian:	n/a
14	chr19:21933459-21933509	ProgFib	skin:	n/a
15	chr19:21933450-21933500	GM12892	blood:	n/a
16	chr19:21933455-21933505	PrEC	prostate:	n/a
17	chr19:21933459-21933509	SKMC	muscle:	n/a
18	chr19:21933459-21933509	HEK293	kidney:	embryo
19	chr19:21933455-21933505	AG09309	skin:	n/a
20	chr19:21933455-21933505	HCT-116	colon:	n/a
21	chr19:21933455-21933505	MCF10A-Er-Src	breast:	n/a
22	chr19:21933450-21933500	NB4	blood:	n/a
23	chr19:21933455-21933505	H1-hESC	embryonic stem cell:	embryo
24	chr19:21933450-21933500	HMEC	breast:	n/a
25	chr19:21933455-21933505	Hela-S3	cervix:	n/a
26	chr19:21933459-21933509	K562	blood:	n/a
27	chr19:21933455-21933505	SKMC	muscle:	n/a
28	chr19:21933455-21933505	BE2_C	brain:	n/a
29	chr19:21933450-21933500	PrEC	prostate:	n/a
30	chr19:21933455-21933505	T-47D	breast:	n/a
31	chr19:21933459-21933509	Jurkat	blood:	n/a
32	chr19:21933450-21933500	BE2_C	brain:	n/a
33	chr19:21933455-21933505	NH-A	brain:	n/a
34	chr19:21933455-21933505	NT2-D1	testis:	n/a
35	chr19:21933450-21933500	AG04449	skin:	fetal
36	chr19:21933459-21933509	A549	lung:	n/a
37	chr19:21933459-21933509	SK-N-MC	brain:	n/a
38	chr19:21933450-21933500	T-47D	breast:	n/a
39	chr19:21933459-21933509	HEEpiC	esophagus:	n/a
40	chr19:21933455-21933505	SK-N-SH_RA	brain:	n/a
41	chr19:21933459-21933509	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:21933459-21933509	RPTEC	kidney:	n/a
43	chr19:21933455-21933505	HIPEpiC	eye:	n/a
44	chr19:21933450-21933500	SAEC	small airway:	n/a
45	chr19:21933459-21933509	CMK	blood:	n/a
46	chr19:21933450-21933500	SK-N-SH_RA	brain:	n/a
47	chr19:21933459-21933509	HCPEpiC	choroid plexus:	n/a
48	chr19:21933450-21933500	IMR90	lung:	fetal
49	chr19:21933450-21933500	HRPEpiC	eye:	n/a
50	chr19:21933450-21933500	MCF10A-Er-Src	breast:	n/a

No data

Variant related genes	Relation type
ENSG00000269845	CpG island
ENSG00000265084	CpG island

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs12971855	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12971857	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12972019	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12972529	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12972582	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12972656	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12973310	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12973788	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12973798	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12974150	0.86[EUR][1000 genomes]
rs12974842	0.86[AMR][1000 genomes]
rs12975386	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12975387	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12977947	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12978145	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12979324	0.88[EUR][1000 genomes]
rs12981854	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12982134	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12982588	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12982621	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12983229	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12985617	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12985708	0.86[EUR][1000 genomes]
rs16998300	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28492771	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34063259	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34387769	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34569334	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34617884	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34627818	0.86[EUR][1000 genomes]
rs34632362	0.86[EUR][1000 genomes]
rs34652503	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34906160	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34908429	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34926877	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35161629	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35251105	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35336315	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35358346	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35367448	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35407033	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35409731	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35441629	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35447051	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35451495	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35577863	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35584589	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35587380	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35588095	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35590941	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35621425	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35646356	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35715827	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35725943	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35881881	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35910168	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35923238	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36097084	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36104232	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55694447	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55799773	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55817748	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57394342	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57450176	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58873883	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59556202	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59825581	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60086097	0.86[EUR][1000 genomes]
rs61182414	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61196724	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73928595	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73928772	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs74167876	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs74167877	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74167878	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74167879	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74167880	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74167882	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8107583	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911422	chr19:21752009-21973929	ZNF genes & repeats Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv3441368	chr19:21781459-22182822	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv3339694	chr19:21781479-22182792	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1063115	chr19:21782104-22528039	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
5	nsv458525	chr19:21796943-22019697	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv578969	chr19:21796943-22019697	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic 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	13 gene(s)	inside rSNPs	diseases
7	esv3392559	chr19:21798396-21965956	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv911424	chr19:21798441-22471156	Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
9	nsv833783	chr19:21821406-21991838	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv1815274	chr19:21825750-21981855	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv911425	chr19:21841379-22338142	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv911426	chr19:21892040-21973929	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv911427	chr19:21900898-21960407	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv833784	chr19:21902647-22037153	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic 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	9 gene(s)	inside rSNPs	diseases
15	nsv578970	chr19:21906655-21973929	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv961193	chr19:21911308-21950500	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	esv3342879	chr19:21913482-21968857	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21905600-21947200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:21906200-21949200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:21908800-21948800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
4	chr19:21909200-21946000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:21911200-21935600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr19:21913400-21941200	Weak transcription	NHDF-Ad	bronchial
7	chr19:21914000-21934600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
8	chr19:21916800-21944600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr19:21917200-21934200	Weak transcription	Colon Smooth Muscle	Colon
10	chr19:21918000-21941200	Weak transcription	Brain Angular Gyrus	brain
11	chr19:21918000-21948400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr19:21918800-21934400	Weak transcription	NH-A	brain
13	chr19:21919400-21943800	Strong transcription	Dnd41	blood
14	chr19:21919600-21933800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr19:21920200-21933600	Weak transcription	HUVEC	blood vessel
16	chr19:21920200-21935600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr19:21920200-21949200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:21920400-21948600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr19:21920800-21949200	Weak transcription	NHLF	lung
20	chr19:21921800-21948600	Weak transcription	Stomach Mucosa	stomach
21	chr19:21922000-21933600	Weak transcription	Spleen	Spleen
22	chr19:21922000-21938200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr19:21922000-21941400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr19:21922000-21949400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:21922000-21949400	Weak transcription	HSMMtube	muscle
26	chr19:21922200-21934000	Weak transcription	Brain Hippocampus Middle	brain
27	chr19:21922400-21935600	Weak transcription	HMEC	breast
28	chr19:21922400-21944400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr19:21922400-21945000	Weak transcription	Fetal Kidney	kidney
30	chr19:21922600-21941400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr19:21923800-21934000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr19:21924200-21933800	Weak transcription	Fetal Lung	lung
33	chr19:21925000-21933600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr19:21925000-21933600	Weak transcription	Gastric	stomach
35	chr19:21925000-21933600	Weak transcription	Pancreas	Pancrea
36	chr19:21925000-21934200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr19:21925000-21935000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr19:21925400-21937800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr19:21926000-21933600	Weak transcription	Fetal Intestine Small	intestine
40	chr19:21927000-21933600	Weak transcription	Adipose Nuclei	Adipose
41	chr19:21927000-21933600	Weak transcription	Osteobl	bone
42	chr19:21927000-21933800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr19:21927000-21948400	Weak transcription	HepG2	liver
44	chr19:21927200-21933800	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr19:21927400-21942600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
46	chr19:21927800-21934000	Weak transcription	Fetal Brain Male	brain
47	chr19:21928800-21937000	ZNF genes & repeats	Fetal Brain Female	brain
48	chr19:21928800-21949400	Weak transcription	Psoas Muscle	Psoas
49	chr19:21929200-21948800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
50	chr19:21929600-21936200	ZNF genes & repeats	GM12878-XiMat	blood

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