Variant report

Variant	rs59748816
Chromosome Location	chr6:30135068-30135069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30132800-30135400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:30132800-30136200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:30134400-30135600	Genic enhancers	HepG2	liver
4	chr6:30134600-30139600	Strong transcription	Duodenum Mucosa	Duodenum
5	chr6:30134800-30135200	Enhancers	Primary T cells from cord blood	blood
6	chr6:30134800-30135400	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr6:30134800-30135600	Enhancers	Primary hematopoietic stem cells	blood
8	chr6:30134800-30135600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:30134800-30135600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:30134800-30137000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:30134800-30137400	Strong transcription	Fetal Intestine Large	intestine
12	chr6:30134800-30137400	Strong transcription	Fetal Intestine Small	intestine
13	chr6:30134800-30137600	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr6:30134800-30137800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:30134800-30139600	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr6:30135000-30135200	Bivalent Enhancer	GM12878-XiMat	blood
17	chr6:30135000-30137200	Strong transcription	Colonic Mucosa	Colon
18	chr6:30135000-30137800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr6:30135000-30139000	Strong transcription	Liver	Liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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