Variant report

Variant	esv2762224
Chromosome Location	chr1:228791784-228867656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:228859906-228860016	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:228800055-228800506	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:228791396-228792120	HepG2	liver:	n/a	n/a
4	ATF3	chr1:228799916-228800485	A549	lung:	n/a	n/a
5	BACH1	chr1:228859137-228859199	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:228823025-228823387	GM12878	blood:	n/a	n/a
7	BATF	chr1:228823129-228823328	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:228857269-228857328	K562	blood:	n/a	n/a
9	BRCA1	chr1:228800199-228800448	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:228833066-228833341	IMR90	lung:	n/a	chr1:228833219-228833230
11	CEBPB	chr1:228832992-228833419	MCF-7	breast:	n/a	chr1:228833219-228833230 chr1:228833038-228833055
12	CEBPB	chr1:228814548-228814822	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:228800324-228800601	HepG2	liver:	n/a	chr1:228800436-228800447
14	CEBPB	chr1:228833042-228833401	HepG2	liver:	n/a	chr1:228833219-228833230
15	CEBPB	chr1:228833046-228833408	HepG2	liver:	n/a	chr1:228833219-228833230
16	CEBPB	chr1:228800318-228800526	HepG2	liver:	n/a	chr1:228800436-228800447
17	CEBPB	chr1:228833036-228833345	Hela-S3	cervix:	n/a	chr1:228833219-228833230 chr1:228833038-228833055
18	CEBPB	chr1:228823455-228823652	K562	blood:	n/a	n/a
19	CEBPB	chr1:228799940-228800557	A549	lung:	n/a	chr1:228800436-228800447
20	CEBPB	chr1:228791712-228792122	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:228800284-228800603	HepG2	liver:	n/a	chr1:228800436-228800447
22	CEBPB	chr1:228823299-228823681	K562	blood:	n/a	n/a
23	CEBPB	chr1:228800256-228800601	H1-hESC	embryonic stem cell:	n/a	chr1:228800436-228800447
24	CEBPB	chr1:228833084-228833307	HepG2	liver:	n/a	chr1:228833219-228833230
25	CEBPB	chr1:228800202-228800604	Hela-S3	cervix:	n/a	chr1:228800436-228800447
26	CEBPB	chr1:228833085-228833386	MCF-7	breast:	n/a	chr1:228833219-228833230
27	CEBPB	chr1:228800271-228800600	HepG2	liver:	n/a	chr1:228800436-228800447
28	CEBPB	chr1:228859659-228859972	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:228827707-228827934	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:228833057-228833257	H1-hESC	embryonic stem cell:	n/a	chr1:228833219-228833230
31	CEBPB	chr1:228833080-228833333	A549	lung:	n/a	chr1:228833219-228833230
32	CEBPB	chr1:228800378-228800529	K562	blood:	n/a	chr1:228800436-228800447
33	CEBPB	chr1:228804941-228805118	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:228827800-228827950	HEK293	kidney:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
35	CTCF	chr1:228827760-228827910	A549	lung:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
36	CTCF	chr1:228827820-228827970	HMEC	breast:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
37	CTCF	chr1:228827911-228827934	GM19239	blood:	n/a	n/a
38	CTCF	chr1:228800240-228800390	HEEpiC	esophagus:	n/a	chr1:228800313-228800331 chr1:228800316-228800329 chr1:228800315-228800336
39	CTCF	chr1:228800260-228800410	AoAF	blood vessel:	n/a	chr1:228800313-228800331 chr1:228800316-228800329 chr1:228800315-228800336
40	CTCF	chr1:228827851-228827944	ProgFib	skin:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
41	CTCF	chr1:228800225-228800454	GM19238	blood:	n/a	chr1:228800313-228800331 chr1:228800316-228800329 chr1:228800315-228800336
42	CTCF	chr1:228827805-228827989	Gliobla	brain:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
43	CTCF	chr1:228800234-228800429	MCF-7	breast:	n/a	chr1:228800313-228800331 chr1:228800316-228800329 chr1:228800315-228800336
44	CTCF	chr1:228827813-228827959	GM10266	blood:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
45	CTCF	chr1:228800260-228800410	HUVEC	blood vessel:	n/a	chr1:228800313-228800331 chr1:228800316-228800329 chr1:228800315-228800336
46	CTCF	chr1:228827780-228827930	HRPEpiC	eye:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
47	CTCF	chr1:228827760-228827910	HCM	heart:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
48	CTCF	chr1:228827669-228828055	IMR90	lung:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892
49	CTCF	chr1:228799900-228800050	GM12864	blood:	n/a	n/a
50	CTCF	chr1:228827780-228827930	GM12873	blood:	n/a	chr1:228827877-228827898 chr1:228827875-228827893 chr1:228827878-228827891 chr1:228827876-228827892

No.	Distal block	Cell Line	Cell type
1	chr1:228799860..228800789-chr1:229364053..229364726,2	K562	blood:
2	chr1:228827328..228828298-chr1:229390197..229391242,4	MCF-7	breast:
3	chr1:228849157..228851594-chr1:228855055..228857627,2	MCF-7	breast:
4	chr1:228799820..228800820-chr1:229362779..229363845,6	K562	blood:
5	chr1:228837459..228839753-chr1:228856772..228859694,2	MCF-7	breast:
6	chr1:228860906..228863174-chr1:228870066..228872859,2	MCF-7	breast:
7	chr1:228807843..228809991-chr1:228835972..228838539,2	MCF-7	breast:
8	chr1:228790582..228793514-chr1:229641163..229642685,2	K562	blood:
9	chr1:228849157..228851594-chr1:228855055..228857627,2	MCF-7	breast:
10	chr1:228860050..228863898-chr1:228864456..228870040,6	MCF-7	breast:
11	chr1:228852284..228853865-chr1:228855703..228858059,2	MCF-7	breast:
12	chr1:228827270..228827967-chr1:228870237..228871130,2	MCF-7	breast:
13	chr1:228855647..228857240-chr1:228870729..228872783,2	MCF-7	breast:
14	chr1:228837459..228839753-chr1:228856772..228859694,2	MCF-7	breast:
15	chr1:228800181..228801156-chr1:229390423..229391107,2	MCF-7	breast:
16	chr1:228860160..228864147-chr1:228866037..228871463,5	K562	blood:
17	chr1:228791353..228793996-chr1:228800070..228802504,2	K562	blood:
18	chr1:228827494..228829318-chr1:229289398..229291187,2	MCF-7	breast:
19	chr1:228837388..228839548-chr1:228852852..228854681,2	K562	blood:
20	chr1:228860050..228863898-chr1:228864456..228870040,6	MCF-7	breast:
21	chr1:228791353..228793996-chr1:228800070..228802504,2	K562	blood:
22	chr1:228645146..228646718-chr1:228862119..228864431,2	MCF-7	breast:
23	chr1:228827541..228828103-chr1:229155382..229156112,2	MCF-7	breast:
24	chr1:228827403..228828164-chr1:229292298..229292975,4	MCF-7	breast:
25	chr1:228825405..228828312-chr1:229229360..229231011,2	MCF-7	breast:
26	chr1:228827485..228830418-chr1:228872715..228875379,2	MCF-7	breast:
27	chr1:228860160..228864408-chr1:228867084..228871463,4	K562	blood:
28	chr1:228824129..228826926-chr1:228870014..228872584,2	MCF-7	breast:
29	chr1:228808309..228811116-chr1:228867849..228869399,2	MCF-7	breast:
30	chr1:228807843..228809991-chr1:228835972..228838539,2	MCF-7	breast:
31	chr1:228837388..228839548-chr1:228852852..228854681,2	K562	blood:
32	chr1:228799902..228800597-chr1:229390553..229391271,2	MCF-7	breast:
33	chr1:228857222..228859505-chr1:228868902..228871273,2	MCF-7	breast:
34	chr1:228852284..228853865-chr1:228855703..228858059,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOU-4	chr1:228795029-228795209	NONHSAT010052
2	lnc-RHOU-4	chr1:228797731-228797952	NONHSAT010052

Variant related genes	Relation type
FTH1P2	TF binding region
RHOU	TF binding region
ENSG00000116574	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000196890	chromatin interactions
ENSG00000233920	chromatin interactions
ENSG00000236975	chromatin interactions

Extended variants
information (count: 1715 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7544212	chr1:228791784-228791785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139981927	chr1:228791788-228791789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567876434	chr1:228791843-228791844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530612681	chr1:228791899-228791900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550649711	chr1:228791935-228791936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376456752	chr1:228791940-228791941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367670236	chr1:228791965-228791966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143470003	chr1:228791998-228791999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539462189	chr1:228792118-228792119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186818873	chr1:228792137-228792138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191258298	chr1:228792146-228792147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535909805	chr1:228792162-228792163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555887891	chr1:228792163-228792164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182580574	chr1:228792180-228792181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544771350	chr1:228792182-228792183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558201957	chr1:228792248-228792249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs578172185	chr1:228792255-228792256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559697118	chr1:228792308-228792309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545504319	chr1:228792311-228792312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530043647	chr1:228792343-228792344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558879046	chr1:228792351-228792352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187073790	chr1:228792354-228792355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370211830	chr1:228792370-228792371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537776652	chr1:228792402-228792403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541568474	chr1:228792419-228792420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561446574	chr1:228792512-228792513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374578036	chr1:228792608-228792609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530650348	chr1:228792612-228792613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550713070	chr1:228792663-228792664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564243229	chr1:228792679-228792680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533205738	chr1:228792691-228792692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374897257	chr1:228792730-228792731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191550096	chr1:228792731-228792732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566911901	chr1:228792770-228792771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368114880	chr1:228792801-228792802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535846866	chr1:228792815-228792816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182254598	chr1:228792829-228792830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150977860	chr1:228792831-228792832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569358764	chr1:228792854-228792855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144571377	chr1:228792859-228792860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148455109	chr1:228792885-228792886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567895679	chr1:228792906-228792907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111612193	chr1:228792938-228792939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534467414	chr1:228792946-228792947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541403329	chr1:228792956-228792957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7355153	chr1:228792967-228792968	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188953362	chr1:228793005-228793006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57624405	chr1:228793048-228793049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71180801	chr1:228793049-228793050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142396709	chr1:228793092-228793093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228784200-228803000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:228787200-228798800	Weak transcription	A549	lung
3	chr1:228787400-228792800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:228787600-228804600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:228791200-228792000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr1:228791200-228792400	Enhancers	Liver	Liver
7	chr1:228791200-228792400	Enhancers	HepG2	liver
8	chr1:228798800-228799000	Enhancers	A549	lung
9	chr1:228799000-228799200	Flanking Active TSS	A549	lung
10	chr1:228799200-228799800	Weak transcription	A549	lung
11	chr1:228799800-228800000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:228799800-228800200	Enhancers	Fetal Intestine Small	intestine
13	chr1:228799800-228800200	Active TSS	A549	lung
14	chr1:228799800-228800600	Active TSS	Duodenum Mucosa	Duodenum
15	chr1:228799800-228800800	Enhancers	HepG2	liver
16	chr1:228799800-228803400	Enhancers	Placenta	Placenta
17	chr1:228800000-228800200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:228800000-228800200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:228800000-228800200	Enhancers	Aorta	Aorta
20	chr1:228800000-228800600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr1:228800000-228800600	Enhancers	Brain Cingulate Gyrus	brain
22	chr1:228800000-228800600	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr1:228800000-228800800	Enhancers	Liver	Liver
24	chr1:228800000-228801200	Enhancers	Stomach Mucosa	stomach
25	chr1:228800000-228804400	Weak transcription	Right Atrium	heart
26	chr1:228800200-228800400	Flanking Active TSS	A549	lung
27	chr1:228800200-228800600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:228800200-228800600	Enhancers	Brain Substantia Nigra	brain
29	chr1:228800200-228802400	Weak transcription	Fetal Intestine Small	intestine
30	chr1:228800200-228804800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:228800200-228805800	Weak transcription	Aorta	Aorta
32	chr1:228800400-228800600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:228800400-228800800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr1:228800600-228801000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr1:228800600-228804000	Weak transcription	Brain Substantia Nigra	brain
36	chr1:228800600-228804600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr1:228800800-228804200	Weak transcription	HepG2	liver
38	chr1:228801000-228801200	Enhancers	Duodenum Mucosa	Duodenum
39	chr1:228801200-228802400	Weak transcription	Stomach Mucosa	stomach
40	chr1:228801200-228802800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr1:228802400-228803000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr1:228802400-228803000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:228802400-228803200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr1:228802400-228803200	Enhancers	Fetal Muscle Leg	muscle
45	chr1:228802400-228803400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:228802400-228803400	Enhancers	Fetal Intestine Large	intestine
47	chr1:228802400-228803400	Enhancers	Fetal Intestine Small	intestine
48	chr1:228802600-228802800	Enhancers	Stomach Mucosa	stomach
49	chr1:228802800-228804800	Enhancers	Duodenum Mucosa	Duodenum
50	chr1:228803000-228803400	Enhancers	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links